Product Details

SNP ID
rs144455277
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:162267514 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGCAGATGATTTCACCATTTATTT[C/G]ATAGTCGGCACACTTCTTTTGCAGT
Phenotype
MIM: 606951
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
IFIH1 PubMed Links
Additional Information
For this assay, SNP(s) [rs1990760] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
IFIH1
Gene Name
interferon induced with helicase C domain 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022168.3 3264 Missense Mutation CAA,GAA Q955E NP_071451.2

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